rs962369

This is a intron variant variant in the BDNF gene.

GWAS Catalog Trait Associations (5)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

body mass index

Sidorenko J et al. Genetic architecture reconciles linkage and association studies of complex traits. Nature Genetics 56(11):2352-2360 (2024)
Allele T
OR 0.02
p 3.0e-27
N 650,000
Large GWAS
European

diastolic blood pressure

Allele C
OR 0.15
p 3.0e-21
N 1,028,980
Large GWAS
multi-ancestry
Allele C
OR 0.02
p 1.0e-17
N 1,212,859
Large GWAS
European

diverticular disease

Allele C
OR
β 0.005
p 2.0e-14
N 409,728
Large GWAS
European

systolic blood pressure

Allele C
OR 0.01
p 2.0e-11
N 1,212,859
Large GWAS
European
Allele C
OR 0.17
p 1.0e-10
N 1,028,980
Large GWAS
multi-ancestry

mathematical ability

Allele T
OR 0.01
p 4.0e-11
N 811,539
Large GWAS
European

About BDNF

This gene encodes a member of the nerve growth factor family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature protein. Binding of this protein to its cognate receptor promotes neuronal survival in the adult brain. Expression of this gene is reduced in Alzheimer's, Parkinson's, and Huntington's disease patients. This gene may play a role in the regulation of the stress response and in the biology of mood disorders. [provided by RefSeq, Nov 2015]

View all BDNF variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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